Zsolt Holló, Hungary

Egis Pharmaceuticals Plc Center of Biotechnology
Zsolt Hollo is a medical doctor by training, holds a Ph.D in cellular physiology and a master of business administration degree. He has several years of R&D experience in biochemistry, molecular diagnostics, diagnostic product development. His research interest was mechanism and functional characterization of multidrug resistance in cancer. He worked for more than 5 years in molecular diagnostic service laboratories. He is one of the founding scientists of Solvo Biotechnology (a Charles River Company), a pioneer company in the drug transporter / ADME-Tox field. He was Medical Director and Chief Operations Officer at Solvo Biotechnology from 2004 to 2009. He works at EGIS Pharmaceuticals since 2010 as a department head at the biotechnology center. The main focuses are scientific support and managing the contract manufacturing of biosimilar products. Recently, he has been working on developing predictive in vitro diagnostic test systems to predict biological therapy response in chronic inflammatory diseases. LinkedIn profile: linkedin.com/in/zsolt-holló-md-phd-mba-97828a18

Presenter of 1 Presentation

THE EVOLVEMENT OF PRECISION MEDICINE IN AUTOIMMUNE DISEASES: GENOMIC BIOMARKERS PREDICTIVE ON THE RESPONSIVENESS OF INFLIXIMAB IN THE TREATMENT OF RHEUMATOID ARTHRITIS

Session Type
PARALLEL SESSIONS
Date
29.05.2021, Saturday
Session Time
13:30 - 15:30
Room
HALL F
Lecture Time
14:50 - 15:00
Session Icon
Pre Recorded

Abstract

Background and Aims

In rheumatoid arthritis (RA) a portion of patients fail to respond to first biological therapy. Predicting the patient’s responsiveness to the first biological therapy is still an unmet medical need. For non-responder patients, this leads to unnecessary exposure, delay of adequate therapy, disease progression and waste of money for the payer as well.

The aim of our study was to identify the selected gene set as genomic biomarkers to predict month 6 therapeutic response to infliximab (IFX), differentiate between good responders and non-responders.

Methods

In the study we enrolled 217 bio-naive RA patients with moderate-high disease activity RA (DAS28-CRP >3.2), who have responded inadequately to DMARDs and assigned to IFX treatment. Developing our in vitro diagnostic test method for the prediction of IFX treatment responsiveness 250 genes were identified by differential gene expression analyses from NGS RNA-Seq data using various machine learning modelling methods, 44 genes were selected which showed significant differences between non-responders and good responders as biomarkers in patient stratification. The expression of this gene set was analyzed using reverse-transcription and quantitative real-time PCR.

Results

Validation clinical studies confirmed that this selected gene set as genomic biomarkers and a proprietary algorithm may predict month 6 therapeutic response to IFX, discriminating between good responders (reached DAS target value DAS28≤3.2 at 6 month) and non-responders.

Conclusions

Our kit received the CE IVD Medical Device Certificate in December 2020, providing a precision medicine tool to personalize IFX therapy.

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